从细菌蛋白质组的假设蛋白质中挖掘潜在药物靶点的计算机方法

Umairah Natasya Mohd Omeershffudin, Suresh Kumar
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引用次数: 16

摘要

蛋白质由一级、二级、三级和四级结构组成。这些结构是建立在连接氨基酸的基础上的。少于50个氨基酸连接在一起的氨基酸序列称为肽,通常是蛋白质的初级结构因此,初级结构被描述为氨基酸的线性链块。如果氨基酸超过50个,就称为多肽。蛋白质的二级结构被称为“折叠蛋白”,其中多肽折叠成α-螺旋、β-链和随机线圈通过氢键连接C=O和N-H,使结构更稳定,从而折叠结构三级结构被称为蛋白质的三维结构(3D),其中蛋白质结构是折叠的。四级结构指的是蛋白质亚基之间的空间关系或相互作用,也称为个体的多肽链。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In silico approach for mining of potential drug targets from hypothetical proteins of bacterial proteome
Protein consists of four levels structure which is primary, secondary, tertiary and quaternary structure. The structures are built based on the linking amino acids. For sequences of amino acids of lesser than fifty amino acids linked together are known as peptides and are usually the primary structure of the protein.1 Hence, the primary structure is described as linear chain blocks of amino acids. If the amino acids are more than fifty, it is described as polypeptides. Secondary structures of the protein are known as the “folding protein” where the polypeptides are either folded to α-helices, β-strands and random coil.2 The structures are folded by linking the C=O and N-H by hydrogen bonds that make the structures more stable.3 Tertiary structures are known as the whole structure of the protein in a 3-Dimensional shape (3D) of which the protein structures are folded. Quaternary structures are referred to as the spatial relationship or the interaction between the subunits of the protein or also known as the individuals’ polypeptide chain.
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